Evidence map›Paper›PMID 32286677›Full record

ArticleHistology and histopathology2020

Prognostic value of microRNA-20b expression level in patients with prostate cancer.

Rongkui Zhang, Fuwei Li, Yuchong Wang, Ming Yao, Changliang Chi

Abstract read
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In one paragraph

Article in Histology and histopathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. The dual role of microRNA (miR)-20b in cancers: Friend or foe?Cell communication and signaling : CCS · 2023
    Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Rongkui ZhangDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin, PR China.
Fuwei LiOperating Room, China-Japan Union Hospital of Jilin University, Changchun, Jilin, PR China.
Yuchong WangDepartment of Magnetic Resonance, Jilin Province FAW General Hospital, Changchun, Jilin, PR China.
Ming YaoDepartment of Radiology, Jilin Cancer Hospital, Changchun, Jilin, PR China.
Changliang ChiDepartment of Urology Surgery, The First Hospital of Jilin University, Changchun, Jilin, PR China. wangweifengdl@163.com.
Jilin University · CNJilin Province Tumor Hospital · CNPeople 's Hospital of Jilin Province · CNUnion Hospital · CN

Funding

- -
6 · The paper itself

Abstract

backgroundmiR-20b is a member of the miR-106a-363 gene cluster located in the mammalian X chromosome, the larger miR-17 family, and the miR-17-92 and miR-106b-25 gene clusters. Previous studies have indicated that miR-20b may function as oncogene or tumor suppressor in different types of cancers. The present study analyzed the association between miR-20b and clinicopathological characteristics of patients with prostate cancer.

methodsA total of 127 pairs of prostate cancer tissue samples and adjacent prostate tissue samples were collected from April 2013 to March 2018. The associations between miR-20b expression levels and clinicopathological factors were assessed using the χ2‑test. Survival was estimated using the Kaplan-Meier method, and the differences in survival according to miR-20b expression were compared using the log-rank test. Prognostic values of miR-20b expression and clinical outcomes were evaluated by Cox regression analysis.

resultsThe relative expression of miR-20b in prostate cancer tissues was significantly higher than that in adjacent noncancerous prostate tissues (P<0.001). miR-20b expression was observed to be significantly associated with Gleason score (P<0.001), lymph node metastasis (P<0.001), and TNM stage (P=0.002). The log-rank test indicated that patients with increased miR-20b expression experienced poor overall survival (P=0.037). Multivariate Cox regression analysis showed that miR-20b expression level (HR=2.181, 95% CI: 1.772-9.021, P=0.016) was an independent factor in predicting the overall survival of prostate cancer patients.

conclusionThe present study demonstrated that tissue miR-20b expression level could be a promising biomarker of prognosis in prostate cancer.

Indexed as

AgedBiomarkers, TumorHumansMaleMicroRNAsMiddle AgedPrognosisProstatic NeoplasmsBiomarkers, TumorMicroRNAsMIRN20b microRNA, human

Identifiers

PMID32286677
OpenAlexW3016187535

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.